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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814121Generated: November 1, 2026

1-Benzenesulfonyl-2-(2-ethoxycarbonylfuran-5-yl-hydroxymethyl)-5-methylthioindole → 1-Benzenesulfonyl-2-(2-ethoxycarbonylfuran-5-yl-methyl)-5-methylthioindole

https://huagongshe.com/reaction/1814121

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzenesulfonyl-2-(2-ethoxycarbonylfuran-5-yl-hydroxymethyl)-5-methylthioindoleHCID 22504440—
CatalystHCID 178418390HCID 178418390—
SolventAcetic AcidHCID 176—
SolventEthanolHCID 702—
Product1-Benzenesulfonyl-2-(2-ethoxycarbonylfuran-5-yl-methyl)-5-methylthioindoleHCID 2250443052.8%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of the compound obtained in Example 30 (2) (0.3586 g) in ethanol (8 ml), acetic acid (1 ml) and 10% palladium carbon (0.3586 g) were added and the mixture was stirred at 50° C. for 15 hours under hydrogen atmosphere. The reaction solution was filtered. The filtrate was concentrated under reduced pressure. The resulting residue was separated using silica gel column chromatography (hexane:ethyl acetate=1:1) to obtain 0.183 g of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06875770B2
Source datasetuspto-grants-2005_04
ORD IDord-349caa0008124cdfbf2aa66647f63e93
Source noteuspto-grants-2005_04